Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| n | 1 | Job Description: | n | 1 | The Clinical Research Coordinator (CRC) will perform independently or with general direction at the |
| > | fully operational journey level of the series to execute, manage, and coordinate research protocols, | ||||
| > | as directed by the Clinical Research Supervisor and/or Principal Investigator (PI) in the Departmen | ||||
| > | t of Pediatrics; may coordinate the data collection and operations of several concurrent clinical re | ||||
| > | search studies under the guidelines of research protocols, UCSF and regulating agency policies. | ||||
| 2 | The Clinical Research Coordinator (CRC) will perform independently or with general direction at the | ||||
| > | fully operational journey level of the series to execute, manage, and coordinate research protocols, | ||||
| > | as directed by the Clinical Research Supervisor and/or Principal Investigator (PI) in the Departmen | ||||
| > | t of Pediatrics; may coordinate the data collection and operations of several concurrent clinical re | ||||
| > | search studies under the guidelines of research protocols, UCSF and regulating agency policies. The | ||||
| > | CRC’s duties may include, but will not be limited to supporting the management and coordinating the | ||||
| > | tasks of single or multiple clinical research studies, depending on their size and complexity; act a | ||||
| > | s intermediary between services and departments while overseeing data and specimen management; manag | ||||
| > | e and report on study results; create, clean, update, and manage databases and comprehensive dataset | ||||
| > | s and reports; coordinate staff work schedules and assist Clinical Research Supervisor and/or PI wit | ||||
| > | h oversight of other research staff; manage Investigator’s protocols in the Institutional Review Boa | ||||
| > | rd (IRB) online system, as well as renewals and modifications of protocol applications and the imple | ||||
| > | mentation of new studies; participate in the review and writing of protocols to ensure institutional | ||||
| > | review board approval within University compliance; help assure compliance with all relevant regula | ||||
| > | tory agencies; oversee study data integrity; implement and maintain periodic quality control procedu | ||||
| > | res; interface with departments to obtain UCSF approval prior to study initiation; maintain all regu | ||||
| > | latory documents; report study progress to investigators; participate in any internal and external a | ||||
| > | udits or reviews of study protocols. | ||||
| 3 | 2 | ||||
| t | 4 | Qualifications: | t | 3 | The CRC’s duties may include, but will not be limited to supporting the management and coordinating |
| > | the tasks of single or multiple clinical research studies, depending on their size and complexity; | ||||
| > | act as intermediary between services and departments while overseeing data and specimen management; | ||||
| > | manage and report on study results; create, clean, update, and manage databases and comprehensive da | ||||
| > | tasets and reports; coordinate staff work schedules and assist Clinical Research Supervisor and/or P | ||||
| > | I with oversight of other research staff; manage Investigator’s protocols in the Institutional Revie | ||||
| > | w Board (IRB) online system, as well as renewals and modifications of protocol applications and the | ||||
| > | implementation of new studies; participate in the review and writing of protocols to ensure institut | ||||
| > | ional review board approval within University compliance; help assure compliance with all relevant r | ||||
| > | egulatory agencies; oversee study data integrity; implement and maintain periodic quality control pr | ||||
| > | ocedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all | ||||
| > | regulatory documents; report study progress to investigators; participate in any internal and exter | ||||
| > | nal audits or reviews of study protocols. | ||||
| 5 | Required Qualifications: - High School Diploma; or equivalent experience - Attention to detail; stro | ||||
| > | ng interpersonal skills; excellent, effective verbal and written communication skills to coordinate | ||||
| > | with subjects, team members, other departments and outside institutions; and the ability to multi-ta | ||||
| > | sk in a fast-paced environment while working with a diverse subject population - Ability to work wel | ||||
| > | l independently, complete projects in a timely manner, and prioritize multiple projects to ensure th | ||||
| > | e completion of essential tasks by deadlines Preferred Qualifications: - Fluent in Spanish - BA/BS d | ||||
| > | egree with biology coursework included - Two years experience in a clinical research setting - Fluen | ||||
| > | cy in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, | ||||
| > | and modification of protocols through this system - Understanding of patient population to create ra | ||||
| > | pport and a relationship, while also giving insight to what is realistic and appropriate for patient | ||||
| > | participation - Experience with electronic medical records - Knowledge of medical terminology, and/ | ||||
| > | or the ability to apply information to the assessment, interpretation, and processing of medical dat | ||||
| > | a - Experience applying the following regulations and guidelines:- Good Clinical Practice Guidelines | ||||
| > | - Health Information and Accountability Act (HIPAA) - The Protection of Human Research Subjects - C | ||||
| > | HR regulations for recruitment and consent of research subjects - Effective Cash Handling Procedures | ||||
| > | - Environmental Health and Safety Training - Fire Safety Training | ||||